Variant #0000016472 (NC_000005.9:g.149357470del, NM_000112.3:c.255del (SLC26A2))
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.149357470del |
DNA change (hg38) |
g.149977907del |
Published as |
282delC: FS/stop |
ISCN |
- |
DB-ID |
SLC26A2_000007 |
Variant remarks |
Rare French DTD mutation |
Reference |
PubMed: Rossi et al. 2001 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
yes |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Anne Polvi |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Anne Polvi |
Date created |
2012-11-15 14:17:13 +01:00 (CET) |
Date last edited |
2020-06-18 08:52:02 +02:00 (CEST) |

Variant on transcripts
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